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Population pharmacokinetics of bupivacaine in combined lumbar and sciatic nerve block

OBJECTIVES: The primary aim of this study was to establish the population pharmacokinetic (PPK) model of bupivacaine after combined lumbar plexus and sciatic nerve blocks and secondary aim is to assess the effect of patient's characteristics including age, body weight and sex on pharmacokinetic...

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Autores principales: Eljebari, Hanene, Jebabli, Nadia, Salouage, Issam, Gaies, Emna, Lakhal, Mohamed, Boussofara, Mehdi, Klouz, Anis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987191/
https://www.ncbi.nlm.nih.gov/pubmed/24741194
http://dx.doi.org/10.4103/0253-7613.129318
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author Eljebari, Hanene
Jebabli, Nadia
Salouage, Issam
Gaies, Emna
Lakhal, Mohamed
Boussofara, Mehdi
Klouz, Anis
author_facet Eljebari, Hanene
Jebabli, Nadia
Salouage, Issam
Gaies, Emna
Lakhal, Mohamed
Boussofara, Mehdi
Klouz, Anis
author_sort Eljebari, Hanene
collection PubMed
description OBJECTIVES: The primary aim of this study was to establish the population pharmacokinetic (PPK) model of bupivacaine after combined lumbar plexus and sciatic nerve blocks and secondary aim is to assess the effect of patient's characteristics including age, body weight and sex on pharmacokinetic parameters. MATERIALS AND METHODS: A total of 31 patients scheduled for elective lower extremity surgery with combined lumbar and sciatic nerve block using plain bupivacaine 0.5% were included. The total bupivacaine plasma concentrations were measured before injection and after two blocks placement and at selected time points. Monitoring of bupivacaine was made by high performance liquid chromatography (HPLC) with ultraviolet detection. Non-linear mixed effects modeling was used to analyze the PPK of bupivacaine. RESULTS: One compartment model with first order absorption, two input compartments and a central elimination was selected. The Shapiro-Wilks test of normality for normalized prediction distribution errors for this model (P = 0.156) showed this as a valid model. The selected model predicts a population clearance of 930 ml/min (residual standard error [RSE] = 15.48%, IC 95% = 930 ± 282.24) with inter individual variability of 75.29%. The central volume of distribution was 134 l (RSE = 12.76%, IC = 134 ± 33.51 L) with inter individual variability of 63.40%. The absorption of bupivacaine in two sites Ka1 and Ka2 were 0.00462/min for the lumbar site and 0.292/min for the sciatic site. Age, body weight and sex have no effect on the bupivacaine pharmacokinetics in this studied population. CONCLUSION: The developed model helps us to assess the systemic absorption of bupivacaine at two injections sites.
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spelling pubmed-39871912014-04-16 Population pharmacokinetics of bupivacaine in combined lumbar and sciatic nerve block Eljebari, Hanene Jebabli, Nadia Salouage, Issam Gaies, Emna Lakhal, Mohamed Boussofara, Mehdi Klouz, Anis Indian J Pharmacol Research Article OBJECTIVES: The primary aim of this study was to establish the population pharmacokinetic (PPK) model of bupivacaine after combined lumbar plexus and sciatic nerve blocks and secondary aim is to assess the effect of patient's characteristics including age, body weight and sex on pharmacokinetic parameters. MATERIALS AND METHODS: A total of 31 patients scheduled for elective lower extremity surgery with combined lumbar and sciatic nerve block using plain bupivacaine 0.5% were included. The total bupivacaine plasma concentrations were measured before injection and after two blocks placement and at selected time points. Monitoring of bupivacaine was made by high performance liquid chromatography (HPLC) with ultraviolet detection. Non-linear mixed effects modeling was used to analyze the PPK of bupivacaine. RESULTS: One compartment model with first order absorption, two input compartments and a central elimination was selected. The Shapiro-Wilks test of normality for normalized prediction distribution errors for this model (P = 0.156) showed this as a valid model. The selected model predicts a population clearance of 930 ml/min (residual standard error [RSE] = 15.48%, IC 95% = 930 ± 282.24) with inter individual variability of 75.29%. The central volume of distribution was 134 l (RSE = 12.76%, IC = 134 ± 33.51 L) with inter individual variability of 63.40%. The absorption of bupivacaine in two sites Ka1 and Ka2 were 0.00462/min for the lumbar site and 0.292/min for the sciatic site. Age, body weight and sex have no effect on the bupivacaine pharmacokinetics in this studied population. CONCLUSION: The developed model helps us to assess the systemic absorption of bupivacaine at two injections sites. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC3987191/ /pubmed/24741194 http://dx.doi.org/10.4103/0253-7613.129318 Text en Copyright: © Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Eljebari, Hanene
Jebabli, Nadia
Salouage, Issam
Gaies, Emna
Lakhal, Mohamed
Boussofara, Mehdi
Klouz, Anis
Population pharmacokinetics of bupivacaine in combined lumbar and sciatic nerve block
title Population pharmacokinetics of bupivacaine in combined lumbar and sciatic nerve block
title_full Population pharmacokinetics of bupivacaine in combined lumbar and sciatic nerve block
title_fullStr Population pharmacokinetics of bupivacaine in combined lumbar and sciatic nerve block
title_full_unstemmed Population pharmacokinetics of bupivacaine in combined lumbar and sciatic nerve block
title_short Population pharmacokinetics of bupivacaine in combined lumbar and sciatic nerve block
title_sort population pharmacokinetics of bupivacaine in combined lumbar and sciatic nerve block
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987191/
https://www.ncbi.nlm.nih.gov/pubmed/24741194
http://dx.doi.org/10.4103/0253-7613.129318
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